| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42878990-42879158 | Common:2; Rare:50 | ||||
| chr21:42879532-42879680 | Common:3; Rare:44 | ||||
| chr21:42893009-42893342 | Common:5; Rare:114 | ||||
| chr21:42974214-42974625 | Common:1; Rare:155 | ||||
| chr21:43659441-43659644 | Common:1; Rare:66 | ||||
| chr21:43728592-43728905 | Common:3; Rare:81 | ||||
| chr21:43776207-43776612 | Common:5; Rare:142; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789367-43789653 | Common:1; Rare:106 | ||||
| chr21:44339244-44339469 | Common:2; Rare:68 | ||||
| chr21:44425601-44425707 | Rare:46 | ||||
| chr21:44801726-44801890 | Rare:67 | ||||
| chr21:44817974-44818238 | Common:1; Rare:111 | ||||
| chr21:44873626-44874050 | Common:8; Rare:170 | ||||
| chr21:44939865-44940042 | Common:3; Rare:48 | ||||
| chr21:45287828-45288087 | Common:6; Rare:105 |